Canonical Allele Identifier: PA2573165190
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473899
ClinVar RCV Id: RCV001970926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1663Val
CA389037189
NM_000257.4:c.4988C>T